Device recall
Z-1181-2024: Software VERIQA (S070031), version 2.0 and 2.1- Software package for display…
FDA device recall · Class II · PTW-FREIBURG
Key facts
| Recall number (Z-number) | Z-1181-2024 |
|---|---|
| Recall event | 93988 |
| Product | Software VERIQA (S070031), version 2.0 and 2.1- Software package for display, evaluation and digital processing of medical image data sets and treatment plans in radiation oncology. |
| Product code | IYE |
| Recalling firm | PTW-FREIBURG |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K213370 |
| FEI number | 3007360740 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database